medicationControlled

Suvorexant

Also known as: Belsomra

Chemical structure of Suvorexant (PubChem CID 24965990)
Structure via PubChem
Half-life
12 h
Typical timing
bedtime
Food rule
either
Default unit
mg

Overview

Suvorexant, marketed as Belsomra, is a medication primarily used for the treatment of insomnia characterized by difficulties with sleep onset and/or sleep maintenance. It belongs to a class of drugs known as dual orexin receptor antagonists (DORAs). Unlike some traditional sleep medications that work by enhancing general brain inhibition, suvorexant targets a specific neurochemical system involved in wakefulness. It is available as an oral tablet and is classified as a Schedule IV controlled substance in the United States due to its potential for abuse, though this risk is considered low (FDA label, DrugBank). The development of suvorexant represents a novel approach to managing insomnia, focusing on suppressing the wake-promoting signals rather than directly sedating the brain. This mechanism is designed to promote sleep more naturally by allowing the body's intrinsic sleep mechanisms to take over. It was approved by the U.S. Food and Drug Administration (FDA) in 2014. Patients considering suvorexant should have a thorough medical evaluation by a licensed clinician to determine its appropriateness for their specific condition.

Deep dive

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Known interactions

  • Category rule: supplement × medication
    Note

    Some supplements change how the body processes medications (absorption, liver enzymes, or additive effects).

    Specific pairs are checked against a licensed drug database and shown with their own severity. Always confirm with your provider or pharmacist.

  • Category rule: vitamin × medication
    Note

    Certain vitamins interact with specific medications (e.g., vitamin K with blood thinners).

    Specific pairs are checked against a licensed source; confirm with your provider.

  • Compound-pair rule
    Note

    Additive sedation possible.

    Start at low melatonin dose (0.3–1 mg) when combined with prescription sedatives.

Frequently asked

Sources referenced

* U.S. Food and Drug Administration (FDA) label for Belsomra * DrugBank * PubChem * Mayo Clinic * Examine.com * Cochrane Library

Stackwise compiles summaries from publicly available scientific and regulatory references. Always verify important decisions with a licensed clinician.

Related compounds

Others in the medication category or studied for the same goals.

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